- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07641465
Effects of Jive Dance Training on Lower Limb Muscle Strength
The Health-promoting Effects of Ballroom Dancing Courses on Lower Limb Strength, Dynamic Balance, Body Composition, and Working Memory of Hospital Employees
The purpose of this study is to evaluate the effects of a structured, partner-free Jive dance training program on the physical and cognitive health of hospital employees. Healthcare workers often face high-stress environments, irregular shifts, and prolonged physical strain, which can lead to reduced muscle strength, poor body composition, and burnout. This study innovates by designing a solo Jive dance intervention to overcome traditional partnership limitations in workplace wellness programs.
A single-group repeated measures design was used, recruiting 20 hospital employees for an 8-week study. The study was divided into Phase A (4 weeks of self-directed group practice) and Phase B (4 weeks of systematic Jive dance training). Comprehensive assessments were conducted at baseline, week 4, and week 8 to measure body composition, lower limb muscle strength, dynamic balance, working memory, and perceived stress.
Descripción general del estudio
Estado
Intervención / Tratamiento
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Taiwan
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Kaohsiung, Taiwan, Taiwán, 824
- E-Da Cancer Hospital
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-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Currently employed as a full-time or part-time staff member at the hospital.
- Aged between 18 and 65 years.
- Voluntarily willing to participate in the 8-week dance program and complete all sequential phases (Phase A and Phase B).
- Mentally and physically capable of performing moderate-to-high intensity structured exercise (such as solo Jive dancing).
- Able to understand the study protocols and provide written informed consent.
Exclusion Criteria:
- Pre-existing severe musculoskeletal injuries, severe joint degeneration, or acute pain that restricts dancing or weight-shifting movements.
- Uncontrolled cardiovascular diseases (e.g., severe hypertension, arrhythmia, or unstable angina) that render high-intensity aerobic exercise unsafe.
- Current pregnancy or plans to become pregnant during the 8-week intervention period.
- Undergoing regular professional or competitive athletic training that could introduce significant confounding effects to the physical outcomes.
- Any other medical condition, severe cognitive impairment, or physical limitation judged by the investigator to pose a safety risk during exercise or interfere with data collection.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Solo Jive Dance Training Group
All participants in this single group will sequentially undergo two distinct phases over an 8-week period.
Phase A involves 4 weeks of self-directed group practice, which serves as the comparison stage.
This is immediately followed by Phase B, consisting of 4 weeks of a systematic, structured solo Jive dance training program (60 minutes per session) designed to enhance physical and cognitive functions.
|
This intervention features an innovative, partner-free "Solo Jive" ballroom dance curriculum designed to overcome the barrier of partner limitations in traditional workplace wellness programs. Distinct from general dance activities, this program is structured into two sequential 4-week phases: a self-directed group practice phase followed by a highly systematic, supervised professional training phase. The core curriculum emphasizes continuous rhythmic tracking, agility, and fast-paced weight-shifting movements characteristic of Jive, focusing heavily on bilateral lower-limb coordination. It is tailored to address healthcare workers' occupational strains, integrating physical neuromuscular training with cognitive-motor engagement (working memory) to provide a dual-benefit intervention for adult workplace populations. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change in Bilateral Lower Limb Plantar Flexion Muscle Strength
Periodo de tiempo: Baseline (T0), Week 4 (T4), and Week 8 (T8)
|
Lower limb muscle strength (specifically plantar flexion) is measured to evaluate the neuromuscular effects of the systematic Jive dance training.
Measurements are taken using a digital handheld dynamometer.
The recorded values are expressed in pounds (lbs) to capture quantitative changes.
An increase in the measured force values from baseline indicates an improvement in lower limb muscle strength.
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Baseline (T0), Week 4 (T4), and Week 8 (T8)
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: YU LING HSU, Clinical Dietitian, E-Da Cancer Hospital
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- EMRP-114-068
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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